Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATTTGTGTGTTTGCAGATCAGGGAG[C/G]AGAGAAACATGAAGGCACAGGTCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
CNOT10 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
CNOT10 - CCR4-NOT transcription complex subunit 10 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256741.1 | 348 | Missense Mutation | GCA,GGA | A,G 11 | NP_001243670.1 | |
NM_001256742.1 | 348 | Missense Mutation | GCA,GGA | A,G 71 | NP_001243671.1 | |
NM_015442.2 | 348 | Missense Mutation | GCA,GGA | A,G 11 | NP_056257.1 | |
XM_006713084.3 | 348 | Missense Mutation | GCA,GGA | A,G 71 | XP_006713147.1 | |
XM_006713085.3 | 348 | Missense Mutation | GCA,GGA | A,G 71 | XP_006713148.1 | |
XM_011533566.2 | 348 | Missense Mutation | GCA,GGA | A,G 71 | XP_011531868.1 | |
XM_011533567.2 | 348 | Intron | XP_011531869.1 | |||
XM_017006109.1 | 348 | Missense Mutation | GCA,GGA | A,G 11 | XP_016861598.1 | |
XM_017006110.1 | 348 | Missense Mutation | GCA,GGA | A,G 11 | XP_016861599.1 | |
XM_017006111.1 | 348 | Missense Mutation | GCA,GGA | A,G 11 | XP_016861600.1 | |
XM_017006112.1 | 348 | Missense Mutation | GCA,GGA | A,G 11 | XP_016861601.1 |